Serial Postoperative Circulating Tumor DNA Assessment Has Strong Prognostic Value During Long-Term Follow-Up in Patients With Breast Cancer

被引:23
作者
Shaw, Jacqueline A. [1 ]
Page, Karen [1 ]
Wren, Evie [2 ]
de Bruin, Elza C. [3 ]
Kalashnikova, Ekaterina [4 ]
Hastings, Robert [1 ]
McEwen, Rob [3 ]
Zhang, Eddie [4 ]
Wadsley, Marc [1 ]
Acheampong, Emmanuel [1 ]
Renner, Derek [5 ]
Gleason, Kelly L. T. [2 ]
Ambasager, Bana [2 ]
Stetson, Daniel [4 ]
Fernandez-Garcia, Daniel [1 ]
Guttery, David [1 ]
Allsopp, Rebecca C. [1 ]
Rodriguez, Angel [5 ]
Zimmermann, Bernhard [5 ]
Sethi, Himanshu [5 ]
Aleshin, Alexey [5 ]
Liu, Minetta C. [6 ]
Richards, Cathy [7 ]
Stebbing, Justin [2 ]
Ali, Simak [2 ]
Rehman, Farah [8 ]
Cleator, Susan [8 ]
Kenny, Laura [2 ]
Ahmed, Samreen [7 ]
Armstrong, Anne C. [9 ]
Coombes, R. Charles [2 ]
机构
[1] Univ Leicester, Leicester Canc Res Ctr, Leicester, England
[2] Imperial Coll London, Dept Surg & Canc, London, England
[3] AstraZeneca, Oncol R&D Res & Early Dev, Cambridge, England
[4] AstraZeneca, Oncol R&D Res & Early Dev, Waltham, PQ, Canada
[5] Natera Inc, Austin, TX USA
[6] Natera Inc, San Carlos, CA USA
[7] Univ Hosp Leicester NHS Trust, Leicester, England
[8] Imperial Coll Healthcare NHS Trust, London, England
[9] Christie NHS Fdn Trust, Div Canc Sci, Manchester, England
关键词
CTDNA;
D O I
10.1200/PO.23.00456
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PURPOSE Here, we report the sensitivity of a personalized, tumor-informed circulating tumor DNA (ctDNA) assay (Signatera) for detection of molecular relapse during long-term follow-up of patients with breast cancer. METHODS A total of 156 patients with primary breast cancer were monitored clinically for up to 12 years after surgery and adjuvant chemotherapy. Semiannual blood samples were prospectively collected, and analyzed retrospectively to detect residual disease by ultradeep sequencing using ctDNA assays, developed from primary tumor whole-exome sequencing data. RESULTS Personalized Signatera assays detected ctDNA ahead of clinical or radiologic relapse in 30 of the 34 patients who relapsed (patient-level sensitivity of 88.2%). Relapse was predicted with a lead interval of up to 38 months (median, 10.5 months; range, 0-38 months), and ctDNA positivity was associated with shorter relapse-free survival (P < .0001) and overall survival (P < .0001). All relapsing triple-negative patients (n = 7/23) had a ctDNA-positive test within a median of 8 months (range, 0-19 months), while the 16 nonrelapsed patients with triple-negative breast cancer remained ctDNA-negative during a median follow-up of 58 months (range, 8-99 months). The four patients who had negative tests before relapse all had hormone receptor-positive (HR+) disease and conversely, five of the 122 nonrelapsed patients (all HR+) had an occasional positive test. CONCLUSION Serial postoperative ctDNA assessment has strong prognostic value, provides a potential window for earlier therapeutic intervention, and may enable more effective monitoring than current clinical tests such as cancer antigen 15-3. Our study provides evidence that those with serially negative ctDNA tests have superior clinical outcomes, providing reassurance to patients with breast cancer. For select cases with HR+ disease, decisions about treatment management might require serial monitoring despite the ctDNA-positive result.
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页数:11
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